US3940481A - Treatment of hepatic coma with isomaltitol - Google Patents
Treatment of hepatic coma with isomaltitol Download PDFInfo
- Publication number
- US3940481A US3940481A US05/441,888 US44188874A US3940481A US 3940481 A US3940481 A US 3940481A US 44188874 A US44188874 A US 44188874A US 3940481 A US3940481 A US 3940481A
- Authority
- US
- United States
- Prior art keywords
- isomaltitol
- treatment
- hepatic coma
- grams
- coma
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- SERLAGPUMNYUCK-YJOKQAJESA-N 6-O-alpha-D-glucopyranosyl-D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O SERLAGPUMNYUCK-YJOKQAJESA-N 0.000 title claims abstract description 17
- 238000011282 treatment Methods 0.000 title claims abstract description 7
- 208000007386 hepatic encephalopathy Diseases 0.000 title claims description 7
- 206010010075 Coma hepatic Diseases 0.000 title claims description 4
- 201000001059 hepatic coma Diseases 0.000 title claims description 4
- 239000003814 drug Substances 0.000 abstract description 6
- 230000001684 chronic effect Effects 0.000 abstract description 4
- 208000019423 liver disease Diseases 0.000 abstract description 3
- 206010010774 Constipation Diseases 0.000 abstract description 2
- 208000027244 Dysbiosis Diseases 0.000 abstract description 2
- 230000007140 dysbiosis Effects 0.000 abstract description 2
- 201000006549 dyspepsia Diseases 0.000 abstract description 2
- 206010067125 Liver injury Diseases 0.000 abstract 1
- 231100000753 hepatic injury Toxicity 0.000 abstract 1
- 238000011321 prophylaxis Methods 0.000 abstract 1
- 229940124597 therapeutic agent Drugs 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
- 102000009027 Albumins Human genes 0.000 description 5
- 108010088751 Albumins Proteins 0.000 description 5
- 241000700159 Rattus Species 0.000 description 5
- 229910021529 ammonia Inorganic materials 0.000 description 5
- MUPFEKGTMRGPLJ-RMMQSMQOSA-N Raffinose Natural products O(C[C@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@@H](O[C@@]2(CO)[C@H](O)[C@@H](O)[C@@H](CO)O2)O1)[C@@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 MUPFEKGTMRGPLJ-RMMQSMQOSA-N 0.000 description 4
- MUPFEKGTMRGPLJ-UHFFFAOYSA-N UNPD196149 Natural products OC1C(O)C(CO)OC1(CO)OC1C(O)C(O)C(O)C(COC2C(C(O)C(O)C(CO)O2)O)O1 MUPFEKGTMRGPLJ-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- MUPFEKGTMRGPLJ-ZQSKZDJDSA-N raffinose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO[C@@H]2[C@@H]([C@@H](O)[C@@H](O)[C@@H](CO)O2)O)O1 MUPFEKGTMRGPLJ-ZQSKZDJDSA-N 0.000 description 4
- 241001465754 Metazoa Species 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000002560 therapeutic procedure Methods 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- 206010010071 Coma Diseases 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 235000005911 diet Nutrition 0.000 description 2
- 210000003608 fece Anatomy 0.000 description 2
- 210000000936 intestine Anatomy 0.000 description 2
- JCQLYHFGKNRPGE-FCVZTGTOSA-N lactulose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 JCQLYHFGKNRPGE-FCVZTGTOSA-N 0.000 description 2
- 229960000511 lactulose Drugs 0.000 description 2
- PFCRQPBOOFTZGQ-UHFFFAOYSA-N lactulose keto form Natural products OCC(=O)C(O)C(C(O)CO)OC1OC(CO)C(O)C(O)C1O PFCRQPBOOFTZGQ-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000006188 syrup Substances 0.000 description 2
- 235000020357 syrup Nutrition 0.000 description 2
- 239000003826 tablet Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 208000004998 Abdominal Pain Diseases 0.000 description 1
- 241000792859 Enema Species 0.000 description 1
- 206010020575 Hyperammonaemia Diseases 0.000 description 1
- 229930193140 Neomycin Natural products 0.000 description 1
- 206010073261 Ovarian theca cell tumour Diseases 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 210000001015 abdomen Anatomy 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 208000010002 alcoholic liver cirrhosis Diseases 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- -1 ammonium ions Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000000112 colonic effect Effects 0.000 description 1
- 239000012059 conventional drug carrier Substances 0.000 description 1
- 230000037213 diet Effects 0.000 description 1
- 230000000378 dietary effect Effects 0.000 description 1
- 239000007938 effervescent tablet Substances 0.000 description 1
- 239000007920 enema Substances 0.000 description 1
- 229940079360 enema for constipation Drugs 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical class CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- 238000012961 medicinal therapy Methods 0.000 description 1
- 229960004927 neomycin Drugs 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 208000001644 thecoma Diseases 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
- C07H15/08—Polyoxyalkylene derivatives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/30—Artificial sweetening agents
- A23L27/33—Artificial sweetening agents containing sugars or derivatives
- A23L27/34—Sugar alcohols
Definitions
- Hepatopathia specifically chronic hepatopathia, and in particular hepatic encephalopathy, are diseases which hitherto it has proved possible to deal with only to an unsatisfactory degree by medicinal therapy.
- the known medicaments prove ineffective in many cases and in addition it was found that the use thereof sometimes involved risk due to their considerable toxicity.
- lactulose has an advantageous effect in such diseases but exhibits undesirable subsidiary effects inasmuch as it is available only in the form of a syrup mixture having a maximum of 70% lactulose, since it is itself difficult to crystallise.
- raffinose for the purpose mentioned, but this is difficult to produce and excessively costly for practical employment.
- the medium is characterised by an isomaltitol content.
- the medicament according to the invention possesses marked pharmacological efficacy.
- This efficacy consists of a healing and preventive effect in the case of hepatopathy, especially chronic hepatopathy and in particular hepatic encephalopathy, dyspepsia, dysbiosis, and also disturbances in the nourishment of infants, such as infant obstipation, pepsinogenous conditions in infants and the like, and the consequences thereof.
- isomaltitol Since isomaltitol is, on passage through the small intestive, cracked and resorbed to a relatively insignificant extent, the main quantity passes into the large intentine. There, a portion of the isomaltitol is metabolised by the non-pathogenic bacteria, whereby bacteria growth and therewith intentine activity is encouraged. The consequence thereof is that the dry substance quantity excreted in the feces increases absolutely, as does also the bacteria content (albumin content) of the feces, as has been ascertained in feeding tests performed on rats.
- Standard laboratory rats were allowed to feed on Altromin standard feed to the amount desired by the rat with the following results.
- a further portion of the isomaltitol is broken down to organic acids, above all lactic acids, and this results in an observed reduction of the pH value in the final intestine.
- the reduction of the pH value results in hindrance of the activity of the flora responsible for the formation of toxic albumin decomposition products.
- toxic albumin decomposition products such as for example ammonia, phenol bodies and others, play an important part in the emergence of the diseases which can be prevented and combated by means of the medicament according to the invention.
- the medicament according to the invention is especially suitable for oral or rectal delivery and can be prepared in any formulation suitable for the form of delivery selected in each particular instance.
- Application can be effected in pure form or together with conventional pharmaceutical carriers excipients.
- Suitable forms of delivery are for example powders, crystalline substances, instant powders, tablets, granules, lozenges, effervescent tablets, capsules, coated pills, syrup, paste, enemas (clysters) and the like.
- the medium can be combined with further therapeutically active agents, for example with antibiotics, sulphonamides and vitamins. Additionally, it is also possible to add flavour-correcting agents. They may also - with unchanged indication- be processed or contained in foodstuffs, in particular dietetic foodstuffs and foodstuffs for infants and children.
- the dosing employed may be almost optionally determined depending on specific requirements. Actually employed are daily doses between about 20 and 250 g, distributed throughout the day in small individual doses.
- An elderly patient with chronic coma hepaticum due to alcoholic liver cirrhosis is given 150 grams isomaltitol daily per os. With a constant diet (40 grams protein daily), an initially good response is observed. The coma could be overcome in a way which is just as good as with neomycin therapy. Without the therapy, a relapse occurs which could, however, still be controlled again by isomaltitol. EEG-observations confirm the clinical course of the treatment.
- An elderly hospitalized patient with non-characteristic abdominal pains is given barium sulfate for 3 days.
- an X-ray is taken of the empty abdomen from a rear posture, whereafter 20 grams isomalitol are administered. Thereafter, the same amounts of raffinose are administered every 30 minutes for a total period of 180 minutes.
- the calculation of the colonic volume from the X-rays gives a maximum volume increase of 400 ml.
- rats After application of a porto-caval shunt, rats show hyperammonaemia which, in the course of time, increases from a normal value of about 100 ⁇ g./100 ml. to 600 ⁇ g./100 ml.
- isomaltitol For the treatment, 0.6 grams isomaltitol are administered to the animals three times daily for 48 hours by means of a stomach probe. The ammonia level is determined before and after the experiments. The ammonia level sinks markedly, in the case of the administration of isomaltitol.
- a middleaged male patient with hepatic coma, stage III is given a total of 1000 ml. of a 15% aqueous solution of isomaltitol, the pH of which is buffered, divided into three doses over the course of the day, administration at a rapid rate by means of a balloon catheter. After the treatment is carried out, there is observed an improvement of consciousness, an improvement of the EKG, and a reduction of the venous and arterial ammonia level. (Further treatment is by the oral administration of raffinose.)
- isomalitol in doses of 20-150 grams daily, especially of 40-60 grams and advantageously of 46 grams, isomaltitol in 4 tablets (4 individual doses) are spread out over the day. A single dose corresponds to 11.5 grams isomaltitol.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Nutrition Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Isomaltitol has also been discovered to be valuable as a therapeutic agent for chronic obstipation and liver injury, in particular for the treatment and prophylaxis of hepatopathy, dyspepsia, dysbiosis and disturbances in the nourishment of infants, and their consequent phenomena.
Description
Hepatopathia, specifically chronic hepatopathia, and in particular hepatic encephalopathy, are diseases which hitherto it has proved possible to deal with only to an unsatisfactory degree by medicinal therapy. The known medicaments prove ineffective in many cases and in addition it was found that the use thereof sometimes involved risk due to their considerable toxicity. It has also already been found that lactulose has an advantageous effect in such diseases but exhibits undesirable subsidiary effects inasmuch as it is available only in the form of a syrup mixture having a maximum of 70% lactulose, since it is itself difficult to crystallise. It has also already been proposed to employ raffinose for the purpose mentioned, but this is difficult to produce and excessively costly for practical employment.
These disadvantages are obviated on employing the therapeutic medium according to the invention. The medium is characterised by an isomaltitol content.
The medicament according to the invention possesses marked pharmacological efficacy. This efficacy consists of a healing and preventive effect in the case of hepatopathy, especially chronic hepatopathy and in particular hepatic encephalopathy, dyspepsia, dysbiosis, and also disturbances in the nourishment of infants, such as infant obstipation, pepsinogenous conditions in infants and the like, and the consequences thereof.
Since isomaltitol is, on passage through the small intestive, cracked and resorbed to a relatively insignificant extent, the main quantity passes into the large intentine. There, a portion of the isomaltitol is metabolised by the non-pathogenic bacteria, whereby bacteria growth and therewith intentine activity is encouraged. The consequence thereof is that the dry substance quantity excreted in the feces increases absolutely, as does also the bacteria content (albumin content) of the feces, as has been ascertained in feeding tests performed on rats.
Standard laboratory rats were allowed to feed on Altromin standard feed to the amount desired by the rat with the following results.
______________________________________
Type of feed Average mg albumin Percentage
per day quantity mass in of dry
of excre- excrement substance
ment in per day and
in the
g dry animal excrement
weight per
day and
animal
______________________________________
Altromin standard
2.7 403 89
feed
Altromin standard
feed
+ 2.5 g sugar
+ 2.5 g. isomaltite
3.1 703 75
Altromin standard
feed
+ 5 g isomaltitol
3.5 920 66
______________________________________
Due to the increased albumin synthesis, there is absorption of ammonium ions or amines from the intestine content and therewith detoxication thereof.
A further portion of the isomaltitol is broken down to organic acids, above all lactic acids, and this results in an observed reduction of the pH value in the final intestine. In turn, the reduction of the pH value results in hindrance of the activity of the flora responsible for the formation of toxic albumin decomposition products. These toxic albumin decomposition products, such as for example ammonia, phenol bodies and others, play an important part in the emergence of the diseases which can be prevented and combated by means of the medicament according to the invention.
The medicament according to the invention is especially suitable for oral or rectal delivery and can be prepared in any formulation suitable for the form of delivery selected in each particular instance. Application can be effected in pure form or together with conventional pharmaceutical carriers excipients. Suitable forms of delivery are for example powders, crystalline substances, instant powders, tablets, granules, lozenges, effervescent tablets, capsules, coated pills, syrup, paste, enemas (clysters) and the like. The medium can be combined with further therapeutically active agents, for example with antibiotics, sulphonamides and vitamins. Additionally, it is also possible to add flavour-correcting agents. They may also - with unchanged indication- be processed or contained in foodstuffs, in particular dietetic foodstuffs and foodstuffs for infants and children.
Since the medicament according to the invention is non-toxic when used in accordance with prescription in reasonable doses, the dosing employed may be almost optionally determined depending on specific requirements. Actually employed are daily doses between about 20 and 250 g, distributed throughout the day in small individual doses.
Use of raffinose in clinical coma therapy
An elderly patient with chronic coma hepaticum due to alcoholic liver cirrhosis is given 150 grams isomaltitol daily per os. With a constant diet (40 grams protein daily), an initially good response is observed. The coma could be overcome in a way which is just as good as with neomycin therapy. Without the therapy, a relapse occurs which could, however, still be controlled again by isomaltitol. EEG-observations confirm the clinical course of the treatment.
This clinical investigation shows that isomaltitol possesses favorable activity in the case of porto-systemic encephalopathy.
An elderly hospitalized patient with non-characteristic abdominal pains is given barium sulfate for 3 days. On the fourth day, an X-ray is taken of the empty abdomen from a rear posture, whereafter 20 grams isomalitol are administered. Thereafter, the same amounts of raffinose are administered every 30 minutes for a total period of 180 minutes. The calculation of the colonic volume from the X-rays gives a maximum volume increase of 400 ml.
Reduction of the ammonia level in rats with a porto-caval shunt
After application of a porto-caval shunt, rats show hyperammonaemia which, in the course of time, increases from a normal value of about 100μg./100 ml. to 600μ g./100 ml.
For the treatment, 0.6 grams isomaltitol are administered to the animals three times daily for 48 hours by means of a stomach probe. The ammonia level is determined before and after the experiments. The ammonia level sinks markedly, in the case of the administration of isomaltitol.
Rectal administration
A middleaged male patient with hepatic coma, stage III, is given a total of 1000 ml. of a 15% aqueous solution of isomaltitol, the pH of which is buffered, divided into three doses over the course of the day, administration at a rapid rate by means of a balloon catheter. After the treatment is carried out, there is observed an improvement of consciousness, an improvement of the EKG, and a reduction of the venous and arterial ammonia level. (Further treatment is by the oral administration of raffinose.)
Administration of isomalitol in doses of 20-150 grams daily, especially of 40-60 grams and advantageously of 46 grams, isomaltitol in 4 tablets (4 individual doses) are spread out over the day. A single dose corresponds to 11.5 grams isomaltitol.
Claims (3)
1. Method for the treatment of hepatic coma, which method comprises administering enterally to the patient an amount of isomaltitol effective for treating said hepatic coma.
2. The method of claim 1 wherein the isomaltitol is applied at a dosage of about 20 to 250 grams per day.
3. The method of claim 2, wherein the dosage is about 100 grams per day.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DT2307251 | 1973-02-14 | ||
| DE2307251A DE2307251C2 (en) | 1973-02-14 | 1973-02-14 | Medicines used to treat chronic constipation and liver damage |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3940481A true US3940481A (en) | 1976-02-24 |
Family
ID=5871894
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/441,888 Expired - Lifetime US3940481A (en) | 1973-02-14 | 1974-02-12 | Treatment of hepatic coma with isomaltitol |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US3940481A (en) |
| DE (1) | DE2307251C2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4898820A (en) * | 1987-07-27 | 1990-02-06 | Showa Denko Kabushiki Kaisha | Process for production of isomaltulose |
| US5578339A (en) * | 1993-05-06 | 1996-11-26 | Sudzucker Aktiengesellschaft Mannheim/Ochsenfurt | Sweetener, process for its preparation and the use thereof |
| US20020061863A1 (en) * | 1999-05-05 | 2002-05-23 | Srinivas Uppugunduri | Novel, specific inhibitors of acute and chronic inflammation |
| EP2668851A1 (en) * | 2012-05-29 | 2013-12-04 | Ueno Fine Chemicals Industry, Ltd. | Liver function-improving agent |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3705039A (en) * | 1969-07-13 | 1972-12-05 | Hayashibara Co | Low calorie sweetener mixture of maltitol and maltotritol |
| DE2217628B1 (en) * | 1972-04-12 | 1973-10-31 | Sueddeutsche Zucker Ag |
-
1973
- 1973-02-14 DE DE2307251A patent/DE2307251C2/en not_active Expired
-
1974
- 1974-02-12 US US05/441,888 patent/US3940481A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3705039A (en) * | 1969-07-13 | 1972-12-05 | Hayashibara Co | Low calorie sweetener mixture of maltitol and maltotritol |
| DE2217628B1 (en) * | 1972-04-12 | 1973-10-31 | Sueddeutsche Zucker Ag |
Non-Patent Citations (1)
| Title |
|---|
| Wolfrom, J. Am. Chem. Soc. Vol. 74, Feb. 20, 1952 pp. 1062-1064. * |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4898820A (en) * | 1987-07-27 | 1990-02-06 | Showa Denko Kabushiki Kaisha | Process for production of isomaltulose |
| US5578339A (en) * | 1993-05-06 | 1996-11-26 | Sudzucker Aktiengesellschaft Mannheim/Ochsenfurt | Sweetener, process for its preparation and the use thereof |
| US20020061863A1 (en) * | 1999-05-05 | 2002-05-23 | Srinivas Uppugunduri | Novel, specific inhibitors of acute and chronic inflammation |
| US20050090467A1 (en) * | 1999-05-05 | 2005-04-28 | Srinivas Uppugunduri | Novel, specific inhibitors or acute and chronic inflammation |
| US7687476B2 (en) * | 1999-05-05 | 2010-03-30 | Srinivas Uppugunduri | Specific inhibitors of acute and chronic inflammation |
| EP2668851A1 (en) * | 2012-05-29 | 2013-12-04 | Ueno Fine Chemicals Industry, Ltd. | Liver function-improving agent |
| US9155752B2 (en) | 2012-05-29 | 2015-10-13 | Ueno Fine Chemicals Industry, Ltd. | Liver function-improving agent |
Also Published As
| Publication number | Publication date |
|---|---|
| DE2307251A1 (en) | 1974-08-22 |
| DE2307251C2 (en) | 1984-03-29 |
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